146255.1

United Arab Emirates

Congenital hypoparathyroidism; Congenital sensorineural hearing impairment; Unilateral renal hypoplasia

Male

Variant Name	Allele Count	Allele Frequency	Associated Disease	Associated Gene
NM_001002295.1:c.35_36del	1		Hypoparathyroidism, Sensorineural Deafness, and Renal Disease